首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Enhanced electrochemical recognition of double-stranded DNA by using hybridization chain reaction and positively charged gold nanoparticles
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Enhanced electrochemical recognition of double-stranded DNA by using hybridization chain reaction and positively charged gold nanoparticles

机译:通过使用杂交链反应和带正电的金纳米颗粒,增强了对双链DNA的电化学识别

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摘要

Enhanced sequence-specific recognition of double-stranded DNA (dsDNA) was realized by using hybridization chain reaction (HCR) and positively charged gold nanoparticles ((+)AuNPs) dual signal amplification. To construct such a sensor, capture probe was initially assembled onto gold electrode surface. Upon addition of dsDNA, sandwiched DNA complex was formed between the capture probe and the detection probe, then another exposed part of the detection probe opened two alternating DNA hairpins (H-1 and H-2) in turn and initiated HCR to form a double-helix. Meantime, (+)AuNPs were electrostatically adsorbed onto such double-helix to amplify the electrochemical signal. Upon optimal conditions, the electronic signals of ferrocene (Fc) that modified on H1 and H2 increased linearly with increasing dsDNA concentration over the range from 15 pM to 1.0 nM, with a detection limit of 2.6 pM. Moreover, the proposed method showed good sequence specificity for dsDNA recognition. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过使用杂交链反应(HCR)和带正电的金纳米颗粒((+)AuNPs)双信号放大,实现了增强的双链DNA(dsDNA)序列特异性识别。为了构造这样的传感器,首先将捕获探针组装到金电极表面上。添加dsDNA后,在捕获探针和检测探针之间形成了夹心的DNA复合物,然后检测探针的另一个裸露部分依次打开了两个交替的DNA发夹(H-1和H-2),并引发了HCR以形成双链-螺旋。同时,(+)AuNP被静电吸附到这种双螺旋上以放大电化学信号。在最佳条件下,在15 pM至1.0 nM的范围内,在dsDNA浓度上,在H1和H2上修饰的二茂铁(Fc)的电子信号线性增加,检出限为2.6 pM。此外,所提出的方法对于dsDNA识别显示出良好的序列特异性。 (C)2015 Elsevier B.V.保留所有权利。

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